BEUDAMED
    62 results · 49ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    SINGLE-USE CUT/COAG HANDPIECE FOR OPEN SURGERY

    FDA Adverse Event
    Injury ·PLASMA SURGICAL INC.·Product code GEI·August 21, 2014

    UNKNOWN PLASMABLADE DEVICE

    FDA Adverse Event
    Injury ·MEDTRONIC ADVANCED ENERGY, LLC·Product code GEI·October 17, 2017

    UNKNOWN MAE GENERATOR

    FDA Adverse Event
    Injury ·MEDTRONIC ADVANCED ENERGY, LLC·Product code GEI·October 17, 2017

    ERBE APC 2

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·September 27, 2019

    ERBE APC 300

    FDA Adverse Event
    Injury ·ERBE ELECTROMEDIZIN GMBH·Product code GEI·June 25, 2010

    FLOSEAL MATRIX HEMOSTATIC SEALANT

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORP.·Product code LMF·July 2, 2003

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·February 11, 2026

    ENDOWRIST

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·January 10, 2022

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·April 13, 2026

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·April 3, 2026

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·April 30, 2026

    DA VINCI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·September 23, 2021

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·March 30, 2026

    ERBE APC 2

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·February 3, 2017

    ERBE APC 2

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·January 26, 2011

    ERBE APC

    FDA Adverse Event
    Injury ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·November 9, 2012

    ION

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code EOQ·October 30, 2024

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·May 12, 2026

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·March 17, 2026

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·May 15, 2026